Canonical Allele Identifier: CA377489332
Gene: PAPSS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.89487068T>C (hg19) chr10:g.87727311T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727311T>C , CM000672.2:g.87727311T>C GRCh38
NC_000010.10:g.89487068T>C , CM000672.1:g.89487068T>C GRCh37
NC_000010.9:g.89477048T>C NCBI36
NG_012150.1:g.72593T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.908T>C MANE Select ENSP00000406157.1:p.Ile303Thr
ENST00000361175.8:c.893T>C ENSP00000354436.4:p.Ile298Thr
ENST00000456849.1:c.908T>C ENSP00000406157.1:p.Ile303Thr
NM_001015880.1:c.908T>C NP_001015880.1:p.Ile303Thr
NM_004670.3:c.893T>C NP_004661.2:p.Ile298Thr
NM_001015880.2:c.908T>C MANE Select NP_001015880.1:p.Ile303Thr
NM_004670.4:c.893T>C NP_004661.2:p.Ile298Thr
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